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715644000: Glomuvenous malformation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303273015 Glomuvenous malformation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303274014 Glomuvenous malformation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303275010 Hereditary multiple glomangioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303276011 Venous malformations with glomus cells en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303277019 Hereditary vascular malformations featuring the presence of small, multifocal bluish-purple venous lesions involving the skin. May be present at birth, and slowly expand during childhood. New small lesions appear with time. Often painful on palpation and cannot be completely emptied by compression. They are usually multifocal and are located mainly on the extremities, involving the skin and subcutis. Caused by mutations in the gene encoding glomulin and inherited in an autosomal dominant manner. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
981891000172113 glomangioma multiples héréditaires fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
1015791000172111 malformation glomuveineuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
953451000172114 glomuveneuze malformatie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
992211000172113 erfelijke meervoudige glomangiomen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glomuvenous malformation (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Glomuvenous malformation (disorder) Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Glomuvenous malformation (disorder) Is a Hereditary disorder of the integument true Inferred relationship Some
Glomuvenous malformation (disorder) Is a Cutaneous vascular malformation (disorder) false Inferred relationship Some
Glomuvenous malformation (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 1
Glomuvenous malformation (disorder) Occurrence Congenital true Inferred relationship Some 1
Glomuvenous malformation (disorder) Finding site Structure of glomus body (body structure) true Inferred relationship Some 1
Glomuvenous malformation (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Glomuvenous malformation (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Glomuvenous malformation (disorder) Is a Congenital venous malformation of skin (disorder) true Inferred relationship Some
Glomuvenous malformation (disorder) Is a Arterial malformation true Inferred relationship Some
Glomuvenous malformation (disorder) Is a Congenital abnormality of vein true Inferred relationship Some
Glomuvenous malformation (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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